Patent application title: Apparatus and Method for providing a Double Balloon Breast Brachytherapy Device
Lloyd Michael Cutrer (Huntington Beach, CA, US)
BEST MEDICAL INTERNATIONAL, INC.
IPC8 Class: AA61M3604FI
Class name: Radioactive substance applied to body for therapy radioactive substance placed within body (e.g., inhaled, implanted, injected, etc.) by fluid injection of radioactive or enhancing agent through body piercing conduit
Publication date: 2012-07-05
Patent application number: 20120172651
According to one general aspect, there is an double-balloon breast
brachytherapy catheter comprising, an outer-balloon that is filled with a
liquid substance or air via an out-balloon-filler; an inner-balloon that
is filled with a liquid substance or air via an inner-balloon-filler,
wherein the inner-balloon is inserted inside the outer-balloon; a
plurality of radiation-tubes connected to an outside boarder of the inner
balloon; a vacuum-tube that is wrapped around an exterior of the
outer-balloon, wherein the vacuum tube is used to remove human fluids and
air to create a void; and a flexible-shaft is connected to an upper-head,
a proximal-tail and a distal-tip, wherein the upper-head is covered by
the outer-balloon, the inner-balloon, the plurality of radiation-tubes
and the vacuum-tube.
1. A double-balloon breast brachytherapy catheter comprising: an
outer-balloon that is filled with a liquid substance or air via an
out-balloon-filler; an inner-balloon that is filled with a liquid
substance or air via an inner-balloon-filler, wherein said inner-balloon
is inserted inside said outer-balloon; a plurality of radiation-tubes
connected to an outside boarder of said inner balloon; a vacuum-tube that
is wrapped around an exterior of said outer-balloon, wherein the vacuum
tube is used to remove human fluids and air to create a void; and a
flexible-shaft is connected to an upper-head, a proximal-tail and a
distal-tip, wherein said upper-head is covered by said outer-balloon,
said inner-balloon, said plurality of radiation-tubes and said
2. A double-balloon breast brachytherapy catheter of claim 1 further comprising: said inner-balloon-filler increases volume of said inner-balloon that correspond to a change in angle and length of said plurality of radiation-tubes, wherein the change in the angle and the length of said radiation-tubes reduces hot spots and cold spots.
3. A double-balloon breast brachytherapy catheter of claim 1 further comprising: said vacuum-tube is attached to said distal-tip of said double-balloon breast brachytherapy catheter and allows for removal of said vacuum tube by releasing the vacuum-tube from said distal-tip.
4. A double-balloon breast brachytherapy catheter of claim 1 further comprising: said outer-balloon is attached to said upper-head by an outer-ring and an inner-ring, wherein said outer-ring and said inner-ring are connected to opposite ends of said outer-balloon to provide a vacuum enclosure.
5. A double-balloon breast brachytherapy catheter of claim 1 further comprising: said inner-balloon is attached to said upper-head by a mini-outer-ring and a mini-inner-ring, wherein said mini-outer-ring and said mini-inner-ring are connected to opposite ends of said inner-balloon to provide a vacuum enclosure within said outer-balloon.
6. A double-balloon breast brachytherapy catheter of claim 1 further comprising: said proximal-tail contains a plurality of radiation-tubes-filler, wherein said plurality of radiation-tubes-fillers are loaded with radioactive material used to treat unhealthy tissue.
7. A method of treating a patient by operating a double-balloon breast brachytherapy catheter comprising: filling a liquid substance or air via an out-balloon-filler; filling a liquid substance or air via an inner-balloon-filler, wherein said inner-balloon is inserted inside an outer-balloon; altering a plurality of radiation-tubes angles and length by filling said inner-balloon-filler; removing human fluids and air to create a void around said double-balloon breast brachytherapy catheter; inserting a flexible-shaft in a human anatomy that is connected to an upper-head, a proximal-tail and a distal-end, wherein said upper-head is covered by said outer-balloon, said inner-balloon, said plurality of radiation-tubes and a vacuum-tube; and loading radioactive material into said radiation-tubes to provide dose treatment to a patient.
8. A method of claim 7, wherein inserting said flexible-shaft in the human anatomy and then filling said outer-balloon to allow an approximate volume of the human anatomy to treat.
9. A method of claim 8, wherein filling said outer-balloon and thereafter changing the angles and lengths of said radiation-tubes by filling a inner-balloon depending on a treatment plan for a patient.
CROSS REFERENCE TO RELATED APPLICATION
FIELD OF THE INVENTION
 The invention generally relates to a device that allows for a conformal radiation dose distribution by allowing medical personnel to change the position and angle of a radiation source by inflating two balloons whereby inner balloon positions treatment catheters within an outer balloon.
 In diagnosing and treating malignant tumors, medical physicians all over the world have tried to create innovative devices designed to treat cancerous tumors in humans. At one time cancer could only be diagnosed when a tumor was big enough to see or feel. Now sophisticated imaging systems can identify tumors far earlier, often before any symptoms have even appeared thereby allowing for early treatment and potential cure. Over the years many different methods have been developed to treat cancer. For breast cancer, surgical approaches such as radical mastectomies were used to remove the breast, chest muscles and underarm lymph nodes--were occasionally performed as early as the 19th century. The late 1940s brought the modified radical mastectomy, which spared the muscle tissue of the patient. In the 1970s, a more limited surgical option came into use, known as Breast Conservation Surgery, which focused on removal of the tumor and a small amount of surrounding tissue commonly referred to as a lumpectomy. In 1985, the lumpectomy combined with whole breast radiation therapy was found to be as effective as the mastectomy in terms of survival rates, but resulted in higher local relapse rates. As a result, medical research looked to provide other forms of combined surgical and localized radiation treatment options.
 At the beginning of the 20th century, shortly after radiation began to be used for diagnosis and therapy, it was discovered that radiation could cause cancer as well as cure it. Many early radiologists used the skin of their arms to test the strength of radiation from their radiotherapy machines, looking for a dose that would produce a pink reaction (erythema) that looked like sunburn. They called this the "erythema dose," and this was considered an estimate of the proper daily fraction of radiation. In retrospect, it is no surprise that many developed leukemia.
 Today, a lumpectomy is a common surgical procedure designed to remove a discrete lump, usually a benign or malignant tumor from an affected woman's breast or in rare occasions a man's breast. As the tissue removed is generally quite limited and the procedure relatively non-invasive, compared to a mastectomy, a lumpectomy is considered a viable means of "breast conservation" or "breast preservation" surgery with all the attendant physical and emotional advantages of such an approach.
 In the past a few breast balloon brachytherapy devices have been developed. The most common types available are the Contura® a multi-lumen balloon breast brachytherapy device, and the MammoSite® breast brachytherapy device. Both devices are used in a procedure known as Accelerated Partial Breast Irradiation. Each device contains certain design drawbacks which will be described in the detail below.
 An example of a brachytherapy applicator may be the "MammoSite® Radiation Therapy System" developed by Proxima Therapeutics, Inc., Alpharetta, Ga. 30005 USA. The MammoSite® RTS, is a balloon catheter which is used in a high dose rate radiation procedure, was introduced specially for use in partial breast irradiation. The MammoSite catheter is inserted at the time of lumpectomy or within 30 days following surgery, remains in place during treatment and is deflated and removed at the end of treatment with mild pain medication. A solid radiation source is typically used; however, a liquid radiation source may also be used with a balloon device placed within a body cavity (e.g., Iotrex®, Proxima Therapeutics, Inc.) The solid radiation source may be removed following each treatment session, with the liquid source remaining in place as long as the balloon remains within the body cavity.
 Clinical trials have shown efficacy of inflatable treatment delivery devices and systems such as MammoSite® RTS and similar devices and systems (e.g., GliaSite® RTS (Proxima Therapeutics, Inc.). However, radiation treatment delivered via these devices and systems can have deleterious effects on healthy tissue while providing the desired effects on cancerous tissue due to limited dose optimization inherent in the design. In a radiation treatment, care must be taken to direct the maximum therapeutic dose to diseased tissue while minimizing radiation dose to healthy tissue. For example, radiation treatment may be most effective when all surrounding tissue regions receive the same dose of radiation, and where the radiation dosage received by more distant tissue is as small and as uniform as possible. However because tissue cavities typically are not uniform or regular in their sizes or shapes and may be near critical structures such as skin, lung, or heart, radiation delivered via the aforementioned inflatable delivery devices can result in less than optimal dosages to different regions of surrounding tissue, creating "hot spots" and regions of relatively low dosage "cold spots".
 In an effort to address this problem, another inventor has developed devices and systems to effectively draw adjacent tissue near a treatment device and thus enhance the treatment of the surrounding tissue (U.S. Pat. No. 6,923,754 B1 to Lubock, U.S. Pat. No. 6,955,641 B2 to Lubock). The Lubock patents described devices and systems that utilize vacuum to draw tissue surrounding a body cavity towards a treatment device placed within. The Lubock devices add a sheath or a fluid-permeable enclosure wall and a vacuum conduit to the Mammosite RTS or similar inflatable treatment delivery devices. These added elements create suction around the device, which draws tissue against the device surface within a body cavity, insuring a closer contact between the tissue and the device. Lubock devices claim that they can urge tissue into a desired orientation and position and form a uniform and controlled surface. This control over the distance, spacing, and the amount of tissue contact offers some advantages to the treatment of lining a body cavity.
 However, despite small improvements, Lubock patents like the other prior arts, failed to provide physicians with better control over the optimization or shaping of the radiation dose within a body cavity. A common shortcoming of these applicators is that the source can only travel in or near a central catheter our centralize set of catheters within a cylindrical, or spherical balloon applicator. The existing balloon catheters only allow an offset from the center shaft of approximately 0 mm to 5 mm. Such designs limit the ability to maximize dose conformality and homogeneity which can only be maximized by allowing the treatment catheters to be placed significantly farther away for the central position. For example, after a surgery, doctors may find that the cavity wall is near sensitive regions which may have a higher sensitivity to radiation damage, including development of new cancerous tissue, than other areas surrounding the resection cavity. Doctors are always looking to deliver the maximum prescribed dose to the target region while minimizing dose to critical structures. Therefore, there is a need in the art to move the treatment catheters farther away from the central shaft of the balloon device will provide enhanced dose conformality, or dose shaping, allowing for greater flexibility in dose delivery to both target structures as well as those regions where reduced dose would be beneficial.
 Design of intra-cavity applicators for brachytherapy is a challenging process, as the bio-mechanical and radiation dosimetry properties of the applicators must be such that they minimize the trauma to the patient during applicator insertion process; that they allow optimal radiation dose conformality to the tumor tissues; and that they provide adequate mechanical strength such that the location of the applicator is predictable throughout the course of treatment. Developments in medical imaging, such as CT, MRI, and PET imaging, have provided clinicians with means to identify tumors on patient images at earlier stages with increased confidence. The technical means to deliver this enhanced conformal dose however is currently severely limited by the available applicators. The present invention aims to overcome these limitations in order to achieve optimal radiation dose distribution to a variety of tumors in or near body cavities.
SUMMARY OF INVENTION
 According to one general aspect, there is an double-balloon breast brachytherapy catheter comprising, an outer-balloon that is filled with a liquid substance or air via an out-balloon-filler; an inner-balloon that is filled with a liquid substance or air via an inner-balloon-filler, wherein the inner-balloon is inserted inside the outer-balloon; a plurality of radiation-tubes connected to an outside boarder of the inner balloon; a vacuum-tube that is wrapped around an exterior of the outer-balloon, wherein the vacuum tube is used to remove human fluids and air to create a void; and a flexible-shaft is connected to an upper-head, a proximal-tail and a distal-tip, wherein the upper-head is covered by the outer-balloon, the inner-balloon, the plurality of radiation-tubes and the vacuum-tube. The double-balloon breast brachytherapy catheter of further comprising, the inner-balloon-filler increases volume of the inner-balloon that correspond to a change in angle and length of the plurality of radiation-tubes, wherein the change in the angle and the length of the radiation-tubes reduces hot spots and cold spots. The double-balloon breast brachytherapy catheter further comprising, the vacuum-tube is attached to the distal-tip of the double-balloon breast brachytherapy catheter and allows for removal of the vacuum tube by releasing the vacuum-tube from the distal-tip. The double-balloon breast brachytherapy catheter of claim 1 further comprising: the outer-balloon is attached to the upper-head by an outer-ring and an inner-ring, wherein the outer-ring and the inner-ring are connected to opposite ends of the outer-balloon to provide a vacuum enclosure. The double-balloon breast brachytherapy catheter further comprising, the inner-balloon is attached to the upper-head by a mini-outer-ring and a mini-inner-ring, wherein the mini-outer-ring and the mini-inner-ring are connected to opposite ends of the inner-balloon to provide a vacuum enclosure within the outer-balloon. The double-balloon breast brachytherapy catheter of claim 1 further comprising, the proximal-tail contains a plurality of radiation-tubes-filler, wherein the plurality of radiation-tubes-fillers are loaded with radioactive material used to treat unhealthy tissue.
 In another aspect, there is a method of treating a patient by operating a double-balloon breast brachytherapy catheter comprising, filling a liquid substance or air via an out-balloon-filler; filling a liquid substance or air via an inner-balloon-filler, wherein the inner-balloon is inserted inside an outer-balloon; altering a plurality of radiation-tubes angles and length by filling the inner-balloon-filler; removing human fluids and air to create a void around the double-balloon breast brachytherapy catheter; inserting a flexible-shaft in a human anatomy that is connected to an upper-head, a proximal-tail and a distal-end, wherein the upper-head is covered by the outer-balloon, the inner-balloon, the plurality of radiation-tubes and a vacuum-tube; and loading radioactive material into the radiation-tubes to provide dose treatment to a patient. The method of treating a patient wherein inserting the flexible-shaft in the human anatomy and then filling the outer-balloon to allow an approximate volume of the human anatomy to treat. The method of treating a patient, wherein filling the outer-balloon and thereafter changing the angles and lengths of the radiation-tubes by filling an inner-balloon depending on a treatment plan for a patient.
DESCRIPTION OF THE DRAWINGS
 FIG. 1 is an illustration of the prior art for the multi-lumen breast single balloon catheter.
 FIG. 2 is an illustration of the internal structure of the shaft in the double-balloon breast catheter without the vacuum outer tube.
 FIG. 3 is an illustration of the internal structure of the shaft in the double-balloon breast catheter with the vacuum outer tube.
 FIG. 4 is an illustration of the internal structure of the double-balloon and the illustration of the flexible [dose tubes].
 FIG. 5 is an illustration of the internal balloon fill volume to demonstrate the flexible [dose tubes].
 FIG. 6 is an illustration of the internal balloon fill volume with the outer vacuum tube with a collapsed outer balloon.
 FIG. 7 is an illustration of top and side view of the suction tube.
 FIG. 8 is a flow-chart of the entire procedure for the lumpectomy and how to use the double-breast balloon.
 The invention generally relates to a device that allows for a conformal dose distribution by allowing medical personnel to change the location and angle of the radiation source by inflating two balloons in a catheter.
 The following detailed description is provided to assist the reader in gaining a comprehensive understanding of the methods, apparatuses, and/or systems described herein. Accordingly, various changes, modifications, and equivalents of the systems, apparatuses and/or methods described herein will be suggested to those of ordinary skill in the art. Also, descriptions of well-known functions and constructions may be omitted for increased clarity and conciseness.
 FIG. 2 shows the double-balloon catheter without the suction tube. The double-balloon allows medical personnel to provide an optimized dose distribution to a region of interest. The balloon structure may contain an outer-balloon 8 and an inner-balloon 9. The outer-balloon has a unique outer-balloon-fill port 15. Furthermore, the inner-balloon 9 may also have an inner-balloon-fill port 11. The two fill ports allow medical personnel to control the individual balloon sizes. This gives maximum amount of control for the medical personal to distribute the optimal radiation dose to a patient. In embodiments of devices and methods having features, either balloon walls may comprise, but not limited to, a polymer, such as a biocompatible polymer, preferably a radiation-resistant polymer. Suitable polymers include a polyolefins such as polyethylene and polypropylene, polyurethanes, polyester, polyvinylchloride, polystyrene, thermoplastic polymers such as C-Flex® (consolidated Polymer Technologies, Inc., Clearwater Fla. 33762), block polymers such as Kraton® (Kraton Polymers, Houston Tex. 77208), an ionomer such as Surlyn® (Dupont, Wilmington Del. 19880), nylon, latex rubber, and silicon rubber (e.g. SILASTIC®, Dow Corning, Midland, Mich.). Furthermore, the inner-balloon 9 is shown connected to four treatment catheters however the design could use a greater or lesser number. For illustration purposes, FIG. 2 displays the top-radiation-tube 12 and the bottom-radiation-tube 13. The radiation-tubes will be connected to each other and will be on the outside of the inner-balloon; however, for future modification, the radiation-tubes can also be inserted inside the inner-balloon. However, inserting the radiation-tubes into the inner balloon has great deficiency as described above. A device having features of the invention may further comprise multiple radiation-tubes. The multiple radiation-tubes can come in many different shapes such as a whisk or may come in a form of a helix, where the radiation tubes are shaped in circle form around the shaft. The radiation-tubes may be configured to run longitudinally along the shaft. During inflation of the balloon assemblies, the radiation-tubes may expand in the direction perpendicular to the shaft while spacing equally from each other and thus forming a three-dimensional catheter framework (or catheter assembly) for the balloon assemblies. The catheter framework may be uniform in size or regular in shape, such as a spherical, cylindrical or an elliptical, or may be non-uniform and irregular. A central catheter may also be inserted into the middle of the inner balloon assembly or the catheter framework. During the procedure, the radiation sources may be inserted into one or more of radiation-tubes following insertion into a body cavity. Radiation source may be solid or liquid and may be advanced within radiation-tubes by fluid or other mechanism, such as a wire, to preferred positions within a given radiation tube. The devices having features may be configured to deliver selective dosages of irradiation treatments to different tissue surrounding a body cavity based on the medical treatment needs of a patient. In addition, FIG. 2 has an A-A view. The A-A view illustrates a cross section of the double-balloon catheter bundle. Just for demonstrative purposes, FIG. 2 has 4 radiation-tubes; however, is not limited to this number and many more radiation-tubes can be added. The A-A view has a side-radiation-tube 16, side-radiation-tube 17, top-radiation-tube 12, top-radiation-tube 13, a measurement center 14, and a suction-tube 18. The central radiation tube 14 may also allow medical personnel to insert a MOSFET or linear array to measure the dose that given to the patient.
 FIG. 3 shows the internal structure of the shaft in the double-balloon breast catheter with the suction-tube 18. FIG. 3A shows the top view of the double-balloon catheter with suction-tube 18. The highlighted area shows the side-radiation-tube 16 and the side-radiation-tube 17 with suction-tube 18. The suction-tube 18 is placed outside the outer-balloon and connected to the distal end cap of the double-balloon catheter. The distal end cap allows for the release of the suction-tube 18 during the procedure or after the procedure. The suction-tube 18 is removed by medical personal pulling out the suction-tube 18 separately from the double-balloon catheter. FIG. 3B shows a side view of the double-balloon catheter with the suction-tube 18. The suction-tube 18 contains small holes along the tube. The suction-tube 18 allows for removal of fluid or air in the body while the procedure is being preformed, and further provides that the surrounding skin is pulled tightly against the balloon. For illustration purposes, the suction-tube 18 is on the outside of the outer-balloon 8. The top-radiation-tube 12, bottom-radiation-tube, and two side-radiation tubes are located on the outside of the inner-balloon. By utilizing the suction-tube 18 and inflating the inner-balloon 9 to position the radiation tubes away from the central shaft, the dose distribution from the radiation source(s) can be optimized to provide the best possible treatment plan for the patient. The best distribution is possible by allowing the inner-balloon 9 to change the location and angle of the radiation tubes. The B-B cross-section view allows to demonstrate that the inner-balloon filler 11 and the outer-balloon-filler 15 are located in the center structure. Furthermore, the B-B view also contains the side-radiation-tube 16, top-radiation-tube 12, bottom-radiation-tube 13, side-radiation-tube 17 and suction-tube 18.
 FIG. 4 shows the internal structure of the double-balloon and a cross-section view of the expansion of the inner-balloon that change in angle and location of the radiation tubes when inflated and deflated. The C-C view of the double-balloon catheter shows the radiation tubes. Just for illustration purposes, there are four radiation-tubes, which are not limited to this number only; as the inner-balloon is filled the radiation-tubes begin to move proportional to the increase in the size of the inner-balloon 9. The inner-balloon 9 expansion volume may vary depending on the fill volume of the outer-balloon 8. The change in the size and angle of the radiation tubes allows for a more optimized dose distribution to the patient. The angle measurements of the radiation tubes can be calculated depending on the amount of fluid inserted into the inner-balloon 9. This allows for medical personnel to optimize radiation dose homogeneity and conformality according to the patient's anatomy. In the radiation-tubes, a fluid radiation source may be any solution of radionuclide(s), e.g., a solution of I-125 or I-131. A radioactive fluid can also be produced using slurry of a suitable fluid containing small particles of a solid radionuclide, such as Au-198 or Y-90. Moreover, the radionuclide(s) can be embodied in a gel. One radioactive material useful is Iotrex®, a sterile single use, non-pyrogenic solution containing sodium 3-(125I) iodo-4-hydroxybenzenesulfonate (125I-HBS), available from Proxima Therapeutics, Inc. of Alpharetta, Ga.
 FIG. 5 shows the internal balloon fill volume 20 to demonstrate the flexibility of the radiation tube. The inner balloon is filled using the inside-filler 21. The inner-balloon can be filled with either saline solution, air, or some type of radiation active liquid. The out-filler-balloon 22 is located outside of the inner balloon on the central shaft; since, the out-side-filler 22 fills the entire outer-balloon. The close of up the double breast balloon shows the internal components of the balloon.
 FIG. 6 shows the internal balloon fill volume with the outer vacuum tube 38 on the outer balloon. The outer-vacuum-tube 38 is used to allow removal fluids and air once the catheter is placed in the cavity. The vacuum-tube may conform to the shape of the outer-balloon. For additional functionality, the vacuum-tube 38 may be removed by the medical personnel by pulling on the tube, thus, allowing removal during or following the placement procedure. The vacuum-tube 38 can be attached to the outer-balloon if a design preference is requested by medical personnel; however, vacuum-tube 38 is not limited to being attached. Another design of the catheter can be the vacuum-tube 38 not being attached to the outer-balloon.
 FIG. 7 shows the top and side view of the vacuum-tube. FIG. 7A shows the top view of the outer-vacuum-tube 19. The vacuum-tube 19 has holes along the tube to remove fluids or air that may be in the cavity. This vacuum-tube permits the outer-balloon to be as close to the human skin as possible. The vacuum-tube is then connected to the end cap of the catheter. FIG. 7B shows the side view of the catheter with vacuum-tube. The inner-balloon-locks 25 create a seal for the inner-balloon. The inner-balloon can be inflated without inflation of the outer balloon if need be in very small cavities or where the increase in volume by the outer-balloon may damage or rupture some of the internal tissue. The vacuum-tube is connected to the end cap of the catheter. The vacuum-tube 19 may be released from the end cap by a mechanical lever or button, initiated by the medical personnel.
 FIG. 8 shows a general procedure for the lumpectomy and how to use the double-balloon device. Lumpectomy 27 is the removal of the breast tumor and some of the normal surrounding tissue. Lumpectomy is a form of "breast-conserving" or "breast preservation" surgery. There are several names used for breast-conserving surgery: biopsy, lumpectomy, partial mastectomy, re-excision, quadrantectomy, or wedge resection. Technically, a lumpectomy is a partial mastectomy, because part of the breast tissue is removed. The catheter is initially provided deflated to allow minimal diameter to allow for insertion through a small incision in the breast. After a few days or weeks following the removal of the tumor, the double balloon breast catheter is placed in the resection of cavity 28 and expanded 29. To evaluate the satisfactory deployment and positioning of the device the patient will undergo an imaging procedure such as an MRI or CT, usually performed by the radiation oncologist 31. Depending on the tumor area, the medical personal can inflate the outer-balloon or the inner-balloon 29. If the area removed is large, the medial personal may want to inflate the outer-balloon first; thus, allowing for internal structural support. On the other hand, if the area is small, the medical personal may want to inflate the inner-balloon first to allow the radiation-tubes to be a certain size and thereafter inflate the outer-balloon. The outer-balloon may have grooves along the outer wall. This will allow tissue to seep into the grooves on the outer-balloon wall and not allow the balloon to rotate inside the patient. Once the balloon is fixed, the patient goes to a radiation oncologist for treatment planning 30. The plan will be determined by the radiation oncologist. During this time, the patient will be undergoing a CT or MRI image to evaluate the positioning of the balloon relative to the resection cavity 31. The images will allow the medical personal to make changes or modify the position of the catheter 32. When the catheter is in optimal position inside the human cavity 33, a medical physicist can create a treatment plan for patient with radiation oncologist 34 prescribing the dose. The radiation treatment can vary depending on cavity location relative to other sensitive critical structures. On average, a patient will receive a fractionated treatment typically 2 fractions per day over three to five days of treatment, and one to four hours a day. The double balloon breast catheter will remain in the patient for the entire course of treatment. During the course of treatment the patient may receive daily imaging of the device to make sure no device positioning changes have occurred relative to the original image which was used to plan the case. If changes have occurred adjustments can be made if necessary 35. During the last day, the balloon will be removed of all fluids and extracted from the human cavity.
 A number of exemplary embodiments have been described above. Nevertheless, it will be understood that various modifications may be made. For example, suitable results may be achieved if the described techniques are performed in a different order and/or if components in a described system, architecture, device, or circuit are combined in a different manner and/or replaced or supplemented by other components or their equivalents. Accordingly, other implementations are within the scope of the following claims.
Patent applications by BEST MEDICAL INTERNATIONAL, INC.
Patent applications in class By fluid injection of radioactive or enhancing agent through body piercing conduit
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